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Items: 1 to 20 of 148

1.

Assessment of early bronchiectasis in young children with cystic fibrosis is dependent on lung volume.

Mott LS, Graniel KG, Park J, de Klerk NH, Sly PD, Murray CP, Tiddens HA, Stephen MS; AREST CF..

Chest. 2013 Oct;144(4):1193-8. doi: 10.1378/chest.12-2589.

PMID:
23681147
2.

Progression of early structural lung disease in young children with cystic fibrosis assessed using CT.

Mott LS, Park J, Murray CP, Gangell CL, de Klerk NH, Robinson PJ, Robertson CF, Ranganathan SC, Sly PD, Stick SM; AREST CF..

Thorax. 2012 Jun;67(6):509-16. doi: 10.1136/thoraxjnl-2011-200912. Epub 2011 Dec 26.

PMID:
22201161
3.

PRAGMA-CF. A Quantitative Structural Lung Disease Computed Tomography Outcome in Young Children with Cystic Fibrosis.

Rosenow T, Oudraad MC, Murray CP, Turkovic L, Kuo W, de Bruijne M, Ranganathan SC, Tiddens HA, Stick SM; Australian Respiratory Early Surveillance Team for Cystic Fibrosis (AREST CF)..

Am J Respir Crit Care Med. 2015 May 15;191(10):1158-65. doi: 10.1164/rccm.201501-0061OC.

PMID:
25756857
4.

Automated CT scan scores of bronchiectasis and air trapping in cystic fibrosis.

DeBoer EM, Swiercz W, Heltshe SL, Anthony MM, Szefler P, Klein R, Strain J, Brody AS, Sagel SD.

Chest. 2014 Mar 1;145(3):593-603. doi: 10.1378/chest.13-0588.

5.

What did we learn from two decades of chest computed tomography in cystic fibrosis?

Tiddens HA, Rosenow T.

Pediatr Radiol. 2014 Dec;44(12):1490-5. doi: 10.1007/s00247-014-2964-6. Epub 2014 Aug 28. Review.

PMID:
25164327
6.

Cystic fibrosis: are volumetric ultra-low-dose expiratory CT scans sufficient for monitoring related lung disease?

Loeve M, Lequin MH, de Bruijne M, Hartmann IJ, Gerbrands K, van Straten M, Hop WC, Tiddens HA.

Radiology. 2009 Oct;253(1):223-9. doi: 10.1148/radiol.2532090306. Epub 2009 Aug 25.

PMID:
19710003
7.

HRCT lung abnormalities are not a surrogate for exercise limitation in bronchiectasis.

Edwards EA, Narang I, Li A, Hansell DM, Rosenthal M, Bush A.

Eur Respir J. 2004 Oct;24(4):538-44.

8.

Bronchiectasis and pulmonary exacerbations in children and young adults with cystic fibrosis.

Loeve M, Gerbrands K, Hop WC, Rosenfeld M, Hartmann IC, Tiddens HA.

Chest. 2011 Jul;140(1):178-185. doi: 10.1378/chest.10-1152. Epub 2010 Dec 9.

PMID:
21148242
9.

Validating chest MRI to detect and monitor cystic fibrosis lung disease in a pediatric cohort.

Tepper LA, Ciet P, Caudri D, Quittner AL, Utens EM, Tiddens HA.

Pediatr Pulmonol. 2016 Jan;51(1):34-41. doi: 10.1002/ppul.23328. Epub 2015 Oct 5.

PMID:
26436668
10.

The development of bronchiectasis on chest computed tomography in children with cystic fibrosis: can pre-stages be identified?

Tepper LA, Caudri D, Rovira AP, Tiddens HA, de Bruijne M.

Eur Radiol. 2016 Dec;26(12):4563-4569. Epub 2016 Apr 23.

11.

Assessment of CF lung disease using motion corrected PROPELLER MRI: a comparison with CT.

Ciet P, Serra G, Bertolo S, Spronk S, Ros M, Fraioli F, Quattrucci S, Assael MB, Catalano C, Pomerri F, Tiddens HA, Morana G.

Eur Radiol. 2016 Mar;26(3):780-7. doi: 10.1007/s00330-015-3850-9. Epub 2015 May 30.

PMID:
26024847
12.

Retrospective review of children presenting with non cystic fibrosis bronchiectasis: HRCT features and clinical relationships.

Edwards EA, Metcalfe R, Milne DG, Thompson J, Byrnes CA.

Pediatr Pulmonol. 2003 Aug;36(2):87-93.

PMID:
12833486
13.

Risk factors for bronchiectasis in children with cystic fibrosis.

Sly PD, Gangell CL, Chen L, Ware RS, Ranganathan S, Mott LS, Murray CP, Stick SM; AREST CF Investigators..

N Engl J Med. 2013 May 23;368(21):1963-70.

14.

Distribution of early structural lung changes due to cystic fibrosis detected with chest computed tomography.

Mott LS, Park J, Gangell CL, de Klerk NH, Sly PD, Murray CP, Stick SM; Australian Respiratory Early Surveillance Team for Cystic Fibrosis Study Group..

J Pediatr. 2013 Jul;163(1):243-8.e1-3. doi: 10.1016/j.jpeds.2012.12.042. Epub 2013 Jan 26.

PMID:
23357185
15.

Computed tomography scanning techniques for the evaluation of cystic fibrosis lung disease.

Robinson TE.

Proc Am Thorac Soc. 2007 Aug 1;4(4):310-5. Review.

PMID:
17652492
16.

Diagnosis of bronchiectasis and airway wall thickening in children with cystic fibrosis: Objective airway-artery quantification.

Kuo W, de Bruijne M, Petersen J, Nasserinejad K, Ozturk H, Chen Y, Perez-Rovira A, Tiddens HAWM.

Eur Radiol. 2017 May 18. doi: 10.1007/s00330-017-4819-7. [Epub ahead of print]

PMID:
28523349
17.

Bronchiectasis: functional significance of areas of decreased attenuation at expiratory CT.

Hansell DM, Wells AU, Rubens MB, Cole PJ.

Radiology. 1994 Nov;193(2):369-74.

PMID:
7972745
18.

Bronchiectases at early chest computed tomography in children with cystic fibrosis are associated with increased risk of subsequent pulmonary exacerbations and chronic pseudomonas infection.

Bortoluzzi CF, Volpi S, D'Orazio C, Tiddens HA, Loeve M, Tridello G, Assael BM.

J Cyst Fibros. 2014 Sep;13(5):564-71. doi: 10.1016/j.jcf.2014.03.006. Epub 2014 Apr 13.

19.

Air trapping on chest CT is associated with worse ventilation distribution in infants with cystic fibrosis diagnosed following newborn screening.

Hall GL, Logie KM, Parsons F, Schulzke SM, Nolan G, Murray C, Ranganathan S, Robinson P, Sly PD, Stick SM; AREST CF., Berry L, Garratt L, Massie J, Mott L, Poreddy S, Simpson S.

PLoS One. 2011;6(8):e23932. doi: 10.1371/journal.pone.0023932. Epub 2011 Aug 19.

20.

Multiple-breath inert gas washout and spirometry versus structural lung disease in cystic fibrosis.

Gustafsson PM, De Jong PA, Tiddens HA, Lindblad A.

Thorax. 2008 Feb;63(2):129-34. Epub 2007 Aug 3.

PMID:
17675316

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